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BIOLINE DENTAL IMPLANT SYSTEMS LTD

US

Last updated May 23, 2026

What BIOLINE DENTAL IMPLANT SYSTEMS LTD makes

Bioline Dental Implant Systems Ltd manufactures reusable diamond dental burs and dental implant systems, including guided surgery drills and step drills. Their product line includes FG Dental Burs for precision dental procedures.

The company’s devices are regulated under FDA Class I and Class II classifications, with submissions recorded in the FDA’s 510(k) and UDI registries. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Bioline Dental Implant Systems Ltd manufacture?

Bioline Dental Implant Systems Ltd specializes in dental devices, primarily producing reusable diamond dental burs and dental implant systems. Their product line includes tools like guided surgery drills and step drills, as well as FG Dental Burs designed for precision dental procedures. These devices are engineered for use in oral surgery and restorative dentistry.

Where is Bioline Dental Implant Systems Ltd based?

The company is headquartered in the United States. This location influences its regulatory compliance, as its devices are subject to FDA oversight under U.S. medical device regulations.

Which regulatory registries list Bioline Dental Implant Systems Ltd’s devices?

Bioline Dental Implant Systems Ltd’s devices are recorded in the FDA’s 510(k) premarket notification program and the FDA’s Unique Device Identification (UDI) system. These registries track submissions and compliance for Class I and Class II devices, ensuring traceability and regulatory transparency.

How are Bioline Dental Implant Systems Ltd’s devices classified under FDA regulations?

Bioline Dental Implant Systems Ltd’s devices fall under FDA Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential health impact.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
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Facebook
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
532209134

Catalogue (267)

Page 4 of 6
DeviceModel / ReferenceRegistriesClassStatus
FG Dental Burs 862/018
FDA UDI
Class IActive
Guided Surgery Drill 3.2mm Diameter x 11.5mm Length
FDA UDI
Class IActive
FG Dental Burs 886/014
FDA UDI
Class IActive
FG Dental Burs 830/012
FDA UDI
Class IActive
FG Dental Burs 875K/010
FDA UDI
Class IActive
FG Dental Burs 807/018
FDA UDI
Class IActive
FG Dental Burs 837/010
FDA UDI
Class IActive
FG Dental Burs 848/016
FDA UDI
Class IActive
FG Dental Burs 652/018
FDA UDI
Class IActive
FG Dental Burs 368/023
FDA UDI
Class IActive
Guided Surgery Drill 3.65mm Diameter x 11.5mm Length
FDA UDI
Class IActive
FG Dental Burs 845KR/018
FDA UDI
Class IActive
FG Dental Burs 801/014
FDA UDI
Class IActive
FG Dental Burs 862/016
FDA UDI
Class IActive
FG Dental Burs 817/055
FDA UDI
Class IActive
FG Dental Burs 909/055
FDA UDI
Class IActive
FG Dental Burs 851/012
FDA UDI
Class IActive
FG Dental Burs 859L/016
FDA UDI
Class IActive
Slim Hex Driver 2.1mm 8mm Diameter x 15mm Length
FDA UDI
Class IActive
FG Dental Burs 881/012
FDA UDI
Class IActive
FG Dental Burs 855/012
FDA UDI
Class IActive
FG Dental Burs 801/009
FDA UDI
Class IActive
FG Dental Burs 846/016
FDA UDI
Class IActive
FG Dental Burs 654/016
FDA UDI
Class IActive
Driver Hex 1.25mm long 8mm Diameter x 28.6mm Length
FDA UDI
Class IActive
FG Dental Burs 801L/025
FDA UDI
Class IActive
FG Dental Burs 863/016
FDA UDI
Class IActive
Guided Surgery Drill 2mm Diameter x 11.5mm Length
FDA UDI
Class IActive
Drill Extension 4.5mm Diameter x 28mm Length
FDA UDI
Class IActive
Guided Surgery Drill 4.2mm Diameter x 8mm Length
FDA UDI
Class IActive
FG Dental Burs 845/014
FDA UDI
Class IActive
FG Dental Burs 807/014
FDA UDI
Class IActive
FG Dental Burs 801L/018
FDA UDI
Class IActive
FG Dental Burs 807/012
FDA UDI
Class IActive
FG Dental Burs 863/014
FDA UDI
Class IActive
FG Dental Burs 830/014
FDA UDI
Class IActive
FG Dental Burs 859/018
FDA UDI
Class IActive
Zygomatic Implant Drill 4mm Diameter x 75mm Length
FDA UDI
Class IActive
Surgical Screwdriver 10mm Diameter x 144mm Length
FDA UDI
Class IActive
FG Dental Burs 847KR/018
FDA UDI
Class IActive
Guided Surgery Drill 2.8mm Diameter x 8mm Length
FDA UDI
Class IActive
Trephine Drill 3.8mm Diameter x 36.6mm Length
FDA UDI
Class IActive
FG Dental Burs 379/023
FDA UDI
Class IActive
FG Dental Burs 801/016
FDA UDI
Class IActive
Zygomatic Implant Drill 4mm Diameter x 95mm Length
FDA UDI
Class IActive
Step Drill 1.5mm Diameter x 35.7mm Length
FDA UDI
Class IActive
FG Dental Burs 879/014
FDA UDI
Class IActive
FG Dental Burs 838/012
FDA UDI
Class IActive
Guided Surgery Drill 3.2mm Diameter x 10mm Length
FDA UDI
Class IActive
FG Dental Burs 878K/020
FDA UDI
Class IActive

Related Companies

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Notified Bodies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Bioline Dental Implant Systems Ltd Migdal Tefen Northern · IL FEI 3014329459